Data / Medical devices / China / Foshan Pingchuang Medical Technology Co., Ltd
Foshan Pingchuang Medical Technology Co., Ltd: FDA-registered device maker in Foshan City Guangdong, China, 3 510(k) clearances
Foshan Pingchuang Medical Technology Co., Ltd is registered with the FDA (registration 3014317667) in Foshan City Guangdong, China. It lists 9 device types. The FDA files 3 510(k) clearances under its listings, the newest dated June 17, 2026. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3014317667
- Address
- Building B,Floors 1-4,No.13,Honggang Section,Liandu Avenue,HonggangCommunity,DaliangSubdistrict,ShundeDistrict, Foshan City Guangdong, China, 528312
- Owner or operator
- Foshan PingChuang Medical Technology Co., Ltd (10078371)
- Roles
- Manufacturer
- First device listed
- October 20, 2020
- Registered through
- 2026
- Brand names listed
- BARWAY Hybrid lubricant Silicone & Water Based 3.38fl.oz.(100ml) x 2PCS, Body Lubricant (PC-LU-A, PC-LU-B, PC-LU-C, PC-LU-D, PC-LU-E, PC-LU-F), CC Lottyplay Hybrid personal lubricant 100ml, CC Lottyplay, Water soluble personal lubricant, Model: 5ml, 100ml, Enema Kit, Model: 80ml, 120ml, 150ml, Hybrid personal lubricant (water&silicone), Hybrid personal lubricant (water&silicone), MOD: 100ml, 120ml, 150ml, 180ml, 200ml, 250ml, 300ml, 360ml ,500ml, Hybrid personal lubricant(water&silicone), MOD: 5ml, 8ml, 10ml, 12ml, 15ml, 20ml, 30ml, 50ml, 60ml, 75ml, 90ml and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bag, Ice | KYR | 1 | Manufacturer | accessdata.fda.gov |
| Douche Apparatus, Vaginal, Therapeutic | HED | 1 | Manufacturer | accessdata.fda.gov |
| Elastomer, Silicone, For Scar Management | MDA | 1 | Manufacturer | accessdata.fda.gov |
| Enema Kit | FCE | 1 | Manufacturer | accessdata.fda.gov |
| Fiber, Medical, Absorbent | FRL | 1 | Manufacturer | accessdata.fda.gov |
| Lubricant, Patient | KMJ | 1 | Manufacturer | accessdata.fda.gov |
| Lubricant, Personal | NUC | 2 | Manufacturer | accessdata.fda.gov |
| Media, Coupling, Ultrasound | MUI | 2 | Manufacturer | accessdata.fda.gov |
| Support Gels | JZR | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 17, 2026 | K253255 | Non-Sterile Ultrasound Gel Sterile Ultrasound Gel | MUI | Substantially Equivalent | Foshan Pingchuang Medical Technology Co., Ltd. | accessdata.fda.gov |
| December 15, 2025 | K252935 | Hybrid personal lubricant (water&silicone) (5ml, 8ml, 10ml, 12ml, 15ml, 20ml, 30ml, 50ml, 60ml, 75ml, 90ml, 100ml, 120ml, 150ml, 180ml, 200ml, 250ml, 300ml, 500ml) | NUC | Substantially Equivalent | Foshan Pingchuang Medical Technology Co., Ltd. | accessdata.fda.gov |
| November 18, 2021 | K212104 | Water-soluble Personal Lubricant | NUC | Substantially Equivalent | Foshan Pingchuang Medical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Fiber, Medical, Absorbent
- All makers of Lubricant, Personal
- All makers of Support Gels
- All makers of Media, Coupling, Ultrasound
- All makers of Bag, Ice
- All makers of Douche Apparatus, Vaginal, Therapeutic
Updated June 17, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.